Rehydration of desiccated intertidal brown algae: Release of dissolved organic carbon and water uptake

The release of dissolved organic carbon (DOC) by Ascophyllum nodosum (L.) Le Jol. and Fucus vesiculusus L. during rehydration was investigated after desiccation under experimental conditions. During 30 min of rehydration of plants which had lost up to 70% of their water, A. nodosum released about 2 to 10 mg C/100 g dry weight, while F. vesiculosus released 10 to 50 times more. When dried to water losses exceeding 70%, plants of both species yielded similar amounts of DOC, approximating 2 g C/100 g dry weight. Considerable variance in the amounts of DOC released by individual plant of both species was observed over the whole range of water losses tested. Among the DOC released, the portion of carbohydrate-C was O to 5% with A. nodosum but 2 to 47% with F. vesiculosus. This difference was most pronounced when less than 100 mg C/100 g dry weight were released. A. nodosum regained a smaller percentage of its original weight than F. vesiculosus after 30 min of rehydration when more than 30% of fresh weight were lost during desiccation. Curves were obtained which enable the estimation of water losses in naturally desiccated specimens within 30 min.     

淡水水体溶解有机氮对有毒藻种的生物有效性

溶解有机氮(Dissolved organic nitrogen,DON)是多数天然水体中溶解氮的主要组成部分。天然水体DON是许多微生命体包括有毒藻种的氮营养源,在供水安全以及水体富营养化等方面的生态环境效应不容忽视。文章系统地介绍了淡水水体DON含量与来源、生物有效性与估算方法,以及对有毒藻种生长的影响。DON的来源是影响水体中DON含量动态特征的关键因素。DON来源包括陆地径流,植物碎屑,土壤淋溶液,沉积物释放,大气沉降,藻类、大型植物、细菌与细胞死亡或自我分解,微型及大型浮游动物捕食和排泄、分泌物释放等。研究表明约有12%～72%的DON可迅速被生物所利用,具显著差异,究其原因可能是其来源组成、化学本质(分子质量与极性)、测试生物组成、是否有细菌作用等因素造成的。不同藻种具有不同氮源利用能力,DON对藻类生长具有直接或间接的作用,并可能影响藻类群落结构(有毒藻类成为优势种)。考虑到水环境保护与饮用水安全供水的重要性,未来研究应重视淡水水体DON生物有效性与其化学本质的揭示,尤其是对有毒藻种。     

淡水水体溶解有机氮对有毒藻种的生物有效性

溶解有机氮（Dissolved organic nitrogen,DON）是多数天然水体中溶解氮的主要组成部分。天然水体DON是许多微生命体包括有毒藻种的氮营养源,在供水安全以及水体富营养化等方面的生态环境效应不容忽视。文章系统地介绍了淡水水体DON含量与来源、生物有效性与估算方法,以及对有毒藻种生长的影响。DON的来源是影响水体中DON含量动态特征的关键因素。DON来源包括陆地径流,植物碎屑,土壤淋溶液,沉积物释放,大气沉降,藻类、大型植物、细菌与细胞死亡或自我分解,微型及大型浮游动物捕食和排泄、分泌物释放等。研究表明约有12％～72％的DON可迅速被生物所利用,具显著差异,究其原因可能是其来源组成、化学本质（分子质量与极性）、测试生物组成、是否有细菌作用等因素造成的。不同藻种具有不同氮源利用能力,DON对藻类生长具有直接或间接的作用,并可能影响藻类群落结构（有毒藻类成为优势种）。考虑到水环境保护与饮用水安全供水的重要性,未来研究应重视淡水水体DON生物有效性与其化学本质的揭示,尤其是对有毒藻种。     

Saguenay河溶解有机质光化学生成溶解无机碳的研究

溶解有机质作为水生生态系统中一种重要的活跃的有机组分,对生态系统中的碳循环起到重要的作用.利用模拟太阳光对Saguenay河溶解有机质的光氧化过程模拟,研究了溶解氧浓度、模拟太阳光波长范围和铁浓度对溶解无机碳产量的影响.研究表明,基于空气饱和样品前72 h的溶解无机碳产量1.39 μmol·L-1·h-1,氧气饱和条件下照射的溶解无机碳产量增加了52.5%,而氮气饱和条件下的照射则只有空气饱和样品的10%.实验以Mylar-D、有机玻璃UF-3和有机玻璃UF-4为滤光片研究了波长范围对溶解无机碳产量的影响,近似计算的结果表明UV-B、UV-A和可见光部分分别占无机碳产量的16.5%,55.4%和28.0%,表明溶解无机碳的生成可发生在紫外光无法到达的水体较深区域.铁在光化学催化氧化过程中起重要作用,当总铁浓度达到10 μmol·L-1时,有效的增加了溶解无机碳的生成速率,其生成速率约为初始样品的1.68倍(初始样品中总铁含量为3.2 μmol·L-1).     

Release of photoassimilated carbon as dissolved organic matter by marine phytoplankton

The release of photoassimilated carbon as dissolved organic matter was studied in situ in oligotrophic and eutrophic marine waters and in axenic laboratory cultures. Percentage extracellular release (PER), integrated for the trophogenic zone, ranged from 6 to 12% in eutrophic waters and from 17 to 27% in oligotrophic seas. Most of the algal cultures released low amounts of dissolved organic matter (5%) during exponential growth. The highest levels of PER were observed in surface and deep samples, possibly as a result of elevated photorespiration and senescent cells. The generally lower values for extracellular release reported in this work as compared to other studies may be partly due to improved experimental techniques which minimized previously encountered artifacts.     

Direct measurement of dissolved organic carbon release by phytoplankton and incorporation by microheterotrophs

It is now possible to divide particulate primary production into algal and heterotrophic components without physical separation. This depends on two innovations, the introduction of isotope in the form of labelled dissolved product(s) of primary production and the employment of a data analysis specifically designed for tracer kinetic incorporation experiments. The ¹⁴C technique described by Steemann Nielsen (1952) is inapplicable in the analyses of certain classes of systems and kinetic tracer incorporation experiments must be employed instead. We show that measurement of PDOC production rate requires such kinetic tracer analyses. Measurements made in the laboratory on water taken from 2 m depth in South West Arm of the Port Hacking estuary showed that: (1) the steady-state rate of PDOC production was 0.10 to 0.13 mg C.m^-3.h^-1; (2) the rate of PDOC incorporation into microheterotroph particulate organic carbon was 0.10 to 0.12 mg C.m^-3.h^-1; (3) the rate at which PDOC was respired to CO₂ was 0.001 to 0.003 mg C.m^-3.h^-1. (4) the PDOC makes up only about 0.1% of the total dissolved organic carbon. The size class of particles associated with PDOC production differed from the size class responsible for uptake of PDOC. More than 50% of the PDOC production was associated with particles having a nominal diameter range of 20 to 63 m, while this fraction was responsible for <10% of the incorporation.     

不同有机物料在潮棕壤中有机碳分解进程

用尼龙网袋法研究了特定年度中，不同月份间有机物料在潮棕壤旱田、水田中有机碳分解速率及C／N变化。结果表明，4种物料(玉米秸和玉米根，水稻秸和水稻根)在潮棕壤地区温度、湿度适宜的前3个月(1999年7—月)迅速分解，之后进入缓慢分解阶段，其中根的分解残留率始终高于秸秆。经计算约有2／3的玉米根和稻根腐解产物残留在土壤里；分解至试验结束。所有物料的C/N比都趋于一致，约在10—13之间，与土壤腐殖质的洲比非常相近，说明这些物料已基本完成其腐殖化过程，而成为较稳定的有机组分、这对增加土壤有机质、培肥土壤非常重要。     

土壤溶解有机碳的研究进展

系统地综述了DOC的来源、组成、性质、影响因素、环境效应及测定方法等。尽管关于土壤DOC的研究目前还不完善,至今对DOC的组成、性质等问题都不是很清楚,但现有的研究已经表明,DOC是土壤圈中一种非常活跃的化学物质,它对土壤中化学物质的溶解、吸附、解吸、迁移和毒性等行为均有显著的影响。     

Distinguishing modes of dissolved organic carbon production in marine macrophytes by tracer kinetic analysis

Tracer kinetic analysis of radioisotope incorporation into dissolved organic compounds reveals two distinct patterns of photosynthate release by macroalgae. In experiments employing Sargassum lacerifolium, dissolved organic carbon was produced at a constant rate during light incubations. Steady state rates of production were never achieved in experiments employing either Ecklonia radiata (Turn.) J. Agardh. or Ulva lactuca L. Analysis of the time-varying radioactivity curves obtained in experiments using these algae always resulted in models consistent with dissolved organic carbon production being an autocatalytic process. Preincubation of U. lactuca in the dark resulted in a diminished (ca. 40%) rate of dissolved organic carbon production during the subsequent light incubations. In no case did the radioisotope content of the dissolved organic carbon approach a limiting value, indicating that in contrast to phytoplankton, uptake rates of photosynthate by macroalgae are always less than the rates of production.     

Lack of avoidance of phenolic-rich brown algae by tropical herbivorous fishes

High levels of polyphloroglucinol phenolics in marine brown algae are usually interpreted as a defensive response to herbivory. However, tropical brown algae generally contain very low levels of phenolics, even though herbivory in many tropical systems (e.g. coral reefs) is intense. This apparent paradox would be explained if polyphenolics did not deter tropical herbivores, in which case selection by herbivores for high levels of phenolics in tropical algae would be weak. To examine this hypothesis, in February 1989 we presented mixed assemblages of herbivorous fishes on the Great Barrier Reef with tropical, phenolic-poor brown algae (primarilySargassum spp.) and closely related (conspecifics in one instance) phenolic-rich temperate species. Different species of brown algae were eaten at very different rates, but these differences were not correlated with variation in the phenolic levels among the plants. TLC and NMR analyses showed no evidence of other, non-polar, metabolites in these algae, with the exception of the temperate speciesHomoeostrichus sinclairii. Thus, variation in non-polar metabolites also did not explain the differences in susceptibility to herbivores among these algae. We conclude that the herbivorous fishes studied here were not deterred by phenolic-rich algae, which suggests that levels of phenolics in many tropical algae may generally be low due to their ineffectiveness as defences. However, alternative explanations for the pattern are possible, and these are discussed.     

Release of dissolved organic carbon from the estuarine intertidal macroalga Enteromorpha prolifera

The estuarine macroalga Enteromorpha prolifera was collected from Coos Bay, Oregon, USA during 1981, and its release of photosynthate as dissolved organic carbon (DOC) was studied using ¹⁴C as a tracer. During photosynthesis in 30 S sea water, with a fixation rate averaging 7.37 mg C g^-1 dry wt h^-1, release ranged from 0.13 to 0.57 mg C g^-1 dry wt h^-1 and from 1.65 to 6.23% of total fixed carbon. Release of DOC appears to be linear with time over 3 h. As exposed algae become increasingly desiccated, their photosynthetic rates decline dramatically, but upon reimmersion the highly desiccated algae lose a larger fraction of their fixed carbon than the slightly desiccated algae. This loss comes in a pulse release of DOC over the initial 15 min, followed by declining release rates. The pulse loss due to rainfall is 5 times greater than that due to tidal resubmergence, and may briefly exceed the prior photosynthetic rate. Although lowering the salinity from 30 to 5 does not substantially alter photosynthetic rates, it does increase the DOC release range up to 1.02 mg C g^-1 dry wt h^-1 and 16.10% of fixed carbon. Heterotrophic microbes from the algal habitat readily use the available DOC at about 15% h^-1.     

Dynamics of nitrogen and dissolved organic carbon at the Hubbard brook experimental forest

The factors controlling spatial and temporal patterns in soil solution and streamwater chemistry are highly uncertain in northern hardwood forest ecosystems in the northeastern United States, where concentrations of reactive nitrogen (Nr) in streams have surprisingly declined over recent decades in the face of persistent high rates of atmospheric Nr deposition and aging forests. Reactive nitrogen includes inorganic species (e.g., ammonium [NH4+], nitrate [NO3-]) and some organic forms (e.g., amino acids) available to support the growth of plants and microbes. The objective of this study was to examine controls on the spatial and temporal patterns in the concentrations and fluxes of nitrogen (N) species and dissolved organic carbon (DOC) in a 12-year record of soil solutions and streamwater along an elevational gradient (540-800 m) of a forested watershed at the Hubbard Brook Experimental Forest (HBEF) in the White Mountains of New Hampshire, USA. Dissolved organic N and DOC concentrations were elevated in the high-elevation spruce-fir-white birch (SFB) zone of the watershed, while NO3- was the dominant N species in the lower elevation hardwood portion of the watershed. Within the soil profile, N retention was centered in the mineral horizon, and significant amounts of N were retained between the lower mineral soil and the stream, supporting the idea that near- and in-stream processes are significant sinks for N at the HBEF. Temporal analysis suggested that hydrologic flow paths can override both abiotic and biotic retention mechanisms (i.e., during the non-growing season when most hydrologic export occurs, or during years with high rainfall), there appears to be direct flushing of N from the organic horizons into the stream via horizontal flow. Significant correlations between soil NO3- concentrations, nitrification rates and streamwater NO3- exports show the importance of biological production as a regulator of inorganic N export. The lack of internal production response (e.g., mineralization, nitrification) to a severe ice storm in 1998 reinforces the idea that plant uptake is the dominant regulator of export response to disturbance.     

Release of dissolved organic matter by some marine macrophytes

The amount of photoassimilated carbon released as dissolved organic carbon was investigated for 5 species of benthic marine macrophytes (Thalassia testudinum, Diplanthera wrightii, Acanthophora spicifera, Chondria dasyphylla, and Dictyota dichotoma) and 1 species of pelagic marine macrophyte (Sargassum natans). Release rates ranged between 0.006 and 0.053 mg C g^-1 h^-1. Percent release values ranged from 1.1 to 3.8%. Spermatophytes had slightly lower percent release values than algae. Investigations performed on the ability of release products to be utilized by heterotrophic organisms showed that 20 to 30% of the released organic carbon was assimilated within a 2-h period.     

Pretreatment for dissolved organic nitrogen testing by gas stripping

ABSTRACT

Total dissolved nitrogen (TDN), including dissolved inorganic nitrogen (DIN) and dissolved organic nitrogen (DON), is of significant importance in aquatic systems due to its roles in numerous environmental processes, such as nutrients for agriculture activities, sources for lake and estuary eutrophication, and one of the major factors contributing to disinfection byproduct formation. The distribution and impact of DIN on these processes are relatively well-understood; however, information on DON is extremely limited, as there is no direct method for its quantification. DON is conventionally determined by subtracting DIN from TDN. However, significant errors may be introduced if DIN is the predominant species in samples with high concentrations of TDN. In order to deal with this challenge, pretreatment method for nitrogen gas stripping was investigated using 56 water samples collected from various ecosystems. The results indicated that after nitrogen gas stripping pretreatment, removal % of ammonia nitrogen (NH₃–N) was more than 87.5%, and the ratios of removal of NH₃–N/removal of TDN (β) were over 86.5% for most of 56 samples with high [NH₃–N], indicating a high efficiency for removal of NH₃–N, and that NH₃–N was the predominant nitrogen species removed for the samples with high [NH₃–N]. Therefore, nitrogen gas stripping is an appropriate pretreatment method for DON testing when NH₃–N is the dominant inorganic nitrogen species.     

Influence of physico-chemical properties of soil clay fractions on the retention of dissolved organic carbon

This study investigated the effects of surface functional groups, cation exchange capacity (CEC), surface charge, sesquioxides and specific surface area (SSA) of three soil clay fractions (SCFs) (kaolinite–illite, smectite and allophane) on the retention of dissolved organic carbon (DOC) in soils. Physico-chemical properties of the SCFs before and after removing native carbon and/or sesquioxides were characterised, and the DOC adsorption–desorption tests were conducted by a batch method. Native organic carbon (OC)/sesquioxide removal treatments led to a small change in the CEC values of kaolinite–illite, but significant changes in those of smectite and allophane. The net negative surface charge increased in all samples with an increase in pH indicating their variable charge characteristics. The removal of native OC resulted in a slight increase in the net positive charge on soil clay surfaces, while sesquioxide removal increased the negative charge. Changes in the functional groups on the SCF surfaces contributed to the changes in CEC and zeta potential values. There was a strong relationship (R ² = 0.93, p < 0.05) between the Langmuir maximum DOC adsorption capacity (Q _max) and SSA. The Q _max value also showed a moderately strong relationship (R ² = 0.55, p < 0.05) with zeta potential (at pH 7). Q _max was only poorly correlated with CEC and native OC content. Therefore, along with SSA, the surface charge and functional groups of SCFs played the key role in determining the adsorption affinity and hence retention of DOC in soils.     

不同地质背景下土壤溶解有机碳含量的季节动态及其影响因子

为了解岩溶区和非岩溶区土壤溶解有机碳(DOC)含量及其季节动态是否存在差异,为今后相关研究提供研究依据,作者用0.5mol·L-1K2SO4浸提法分析测定了广西桂林市灵川县潮田乡毛村由泥盆系融县组灰岩(D3r)发育石灰土、砂页岩(D2l)发育红壤中溶解有机碳的含量及其季节动态变化,并分析了其与影响因子的相互关系。结果表明:石灰土中溶解有机碳的质量分数为:19.3675～143.2524mg·kg-1,红壤的为:221.1652～1016.602mg·kg-1,石灰土因其偏碱、高钙镁、高有机质含量的特性而使得DOC含量远低于非岩溶区红壤的含量;石灰土和酸性土DOC含量在秋季都达到最高值,在冬季或春季含量最低;在空间分布上都随土壤深度增加而降低。岩溶区及非岩溶区土壤DOC含量的季节动态变化可以划分为4个阶段:①9—10月高温少雨,植物凋落物增多,DOC含量在一年中最高;②11月-12月,气温迅速降低,微生物活性随之降低,DOC含量下降;③12月底—4月,前期(12月至次年2月)DOC浓度随土壤有机质含量的增加而增加;后期(3—4月)气温回升,降雨频繁,生物复苏,生物活动旺盛,土壤DOC含量迅速增加;④5—8月,高温多雨,DOC转化为CO2释放出来,部分DOC随雨水淋失,土壤中DOC总含量不高。     

岩溶地区土壤溶解有机碳的季节动态及环境效应

对桂林岩溶试验场土壤溶解有机碳(DOC)进行了逐月的观测，结果显示DOC是岩溶生态系统中活跃的有机碳组分，在岩溶地区碳循环中发挥着重要的作用。一年中土壤DOC的变化特征表现为3个阶段：(1)3-7月，随气温升高、降雨量增加，土壤生物活性和新陈代谢能力极大提高，土壤溶解有机碳呈升高趋势；(2)8-11月，气温保持较高的水平，但降雨量偏低，土壤干燥，土壤微生物活性极大地减弱，土壤DOC质量分数全年最低；(3)12月至次年2月，随温度的降低，土壤生物活性逐渐降低，土壤DOC呈缓慢升高趋势，且与土壤微生物量碳之间存在互为消长的关系。土壤碳酸盐岩的溶蚀速率季节变化与土壤DOC之间存在负相关。文章还提出了岩溶地区土壤碳循环模式及DOC在其中的作用。     

Transformation of some dissolved organic compounds by a natural heterotrophic population

Uptake of radioactively labeled glycolic acid, arginine, glutamic acid, and glycine by natural marine bacterial population was rapid and approached a maximum value which was over 90% of the total substrate. Uptake of glucose was rapid, but had a maximum uptake of less than 80%. All substrates except glycolic acid were assimilated to a similar degree (a maximum of more than 30% of the total given substrate). Glycolic acid had a maximum assimilation of less than 10%. The presence of glycolic acid resulted in no extracellular metabolites detectable on a gel permeation column. Between 5 and 10% of the other substrates were transformed and excreted within 72 h by the bacteria. These exudates were both nominally larger and smaller than the given substrates.NORDA publication number: JA 330:008:80     

羟基自由基对不同来源溶解性有机质(DOM)的氧化能力

采用总有机碳分析仪、紫外-可见吸收光谱以及荧光激发-发射光谱(EEMs)对5种不同来源DOM与·OH的反应过程进行了表征,以考察DOM来源和类别对其与·OH反应的影响.结果表明,不同来源DOM与·OH的反应能力存在显著差异,陆源DOM比水源DOM表现出更强的反应能力.DOM与·OH的反应表现为准一级动力学,以DOC变化表征的反应速率常数kDOC与DOM的芳香碳/脂肪碳的比值(Caro/Cali)有较好的相关性,说明芳香性碳可能是·OH的优先反应位点.以光吸收参数Absave表征的衰减速率常数与kDOC也表现出良好的相关性.因来源与类别的差异,不同DOM不仅初始的EEMs存在差别,而且·OH氧化过程中EEMs的变化也表现出显著的不同.